1-Benzothiazolyl-5-acyloxyimidazolidinones

ABSTRACT

This invention discloses new compounds of the formula ##STR1## wherein X is selected from the group consisting of alkyl, halogen, haloalkyl and alkoxy; n is an integer from 0 to 2; R 1  is selected from the group consisting of alkyl, alkenyl, haloalkyl and alkynyl; and R 2  is selected from the group consisting of alkyl, alkenyl, haloalkyl, alkynyl, alkoxyalkyl, cycloalkyl and ##STR2## WHEREIN P IS AN INTEGER FROM 0 TO 2; Y is selected from the group consisting of alkyl, alkenyl, halogen, haloalkyl, alkoxy, alkylthio, nitro and cyano; and m is an integer from 0 to 3.

This invention relates to new compositions of matter and more specifically relates to new chemical compounds of the formula ##STR3## wherein X is selected from the group consisting of alkyl, halogen, haloalkyl and alkoxy; n is an integer from 0 to 2; R¹ is selected from the group consisting of alkyl, alkenyl, haloalkyl and alkynyl; and R² is selected from the group consisting of alkyl, alkenyl, haloalkyl, alkynyl, alkoxyalkyl, cycloalkyl and ##STR4## WHEREIN P IS AN INTEGER FROM 0 TO 2; Y is selected from the group consisting of alkyl, alkenyl, halogen, haloalkyl, alkoxy, alkylthio, nitro and cyano; and m is an integer from 0 to 3.

The compounds of the present invention are useful as herbicides.

In a preferred embodiment of the present invention X is selected from the group consisting of lower alkyl, chlorine, bromine, fluorine, lower chloroalkyl, lower bromoalkyl, trifluoromethyl and lower alkoxy; n is an integer from 0 to 2; R¹ is selected from the group consisting of lower alkyl, lower alkenyl, lower haloalkyl and propargyl; and R² is selected from the group consisting of alkyl of up to 18 carbon atoms, lower alkenyl, lower haloalkyl, propargyl, lower alkoxyalkyl, cycloalkyl of from 3 to 7 carbon atoms and ##STR5## WHEREIN P IS AN INTEGER FROM 0 TO 2; Y is selected from the group consisting of lower alkyl, lower alkenyl, chlorine, bromine, fluorine, lower haloalkyl, lower alkoxy, lower alkylthio, nitro and cyano; and m is an integer from 0 to 3.

The term "lower" as used herein designates a straight or branched carbon chain of up to six carbon atoms.

The compounds of this invention can be prepared by reacting a compound of the formula ##STR6## wherein X, n and R¹ are as heretofore described, with an acid chloride of the formula ##STR7## wherein R² is as heretofore described, in the presence of an acid acceptor such as a tertiary amine. This reaction can be effected by slowly adding the acid chloride of formula III with stirring to a solution of an about equimolar amount of the compound of formula II in an inert organic solvent, in the presence of the acid acceptor, at a temperature of about 10° to 30° C. After the addition is completed, the reaction mixture can be heated at a temperature ranging up to the reflux temperature of the mixture to ensure completion of the reaction. The desired product can then be recovered by first filtering the reaction mixture to remove acid acceptor chloride, followed by stripping off the solvent if the product is soluble therein, or, if formed as a precipitate, by filtration and subsequent washing and purification.

The compounds of this invention can also be prepared by reacting a compound of formula II with an acid anhydride of the formula ##STR8## wherein R² is as heretofore described, in the presence of a catalytic amount of p-toluenesulfonic acid. This reaction can be effected by combining the reactants and the catalyst at room temperature in an inert organic reaction medium and then heating the reaction mixture on a steam bath with stirring for a period of from 1/2 to 4 hours. After this time the reaction mixture can be cooled, and the desired product can be recovered by filtration if formed as a precipitate or upon evaporation of the organic reaction medium if soluble therein. In some instances the acid anhydride can be used as a solvent for the compound of formula II, obviating the use of an inert solvent as the reaction medium. When lower alkanoic anhydrides are used, water can be added to the reaction mixture to precipitate the desired product upon completion of the reaction. The product can then be purified by conventional means such as recrystallization and the like. In some instances the foregoing reaction results in the formation of a mixture of products consisting of the desired compound of this invention and dehydrated starting material of the formula ##STR9## wherein X, n and R¹ are as described. In these instances the desired product can be isolated by fractional precipitation.

The compounds of formula II can be prepared by heating a compound of the formula ##STR10## wherein X, n and R¹ are as heretofore described, in a dilute, aqueous, acidic reaction medium for a period of from about 10 to about 60 minutes. Temperatures of from about 60° C to the reflux temperature of the reaction mixture can be utilized. The reaction medium can comprise a dilute, aqueous inorganic acid such as hydrochloric acid at a concentration of from about 0.5 to about 10 percent. Lower water-miscible alkanols can also be suitably added to the reaction medium to aid in the dissolution of the starting materials. After completion of the reaction the desired product can be recovered upon evaporation of the solvents used if soluble therein or by filtration if formed as a precipitate. This product can then be used as such or can be further purified by standard techniques such as trituration, recrystallization, washing and the like.

The compounds of formula IV can be prepared by reacting a molar amount of an isocyanate dimer of the formula ##STR11## wherein X and n are as heretofore described, with about two molar amounts of a dimethyl acetal of the formula ##STR12## wherein R¹ is as heretofore described. This reaction can be effected by combining the isocyanate dimer of formula VII dissolved in an inert organic solvent such as benzene with the acetal of formula VIII at room temperature and stirring the resulting mixture for a period of about 1/2 to about 4 hours. After this time the reaction mixture can be filtered and the filtrate stripped of solvent to yield the desired product. This product can be used as such or further purified if desired by standard techniques.

The isocyanate dimer of formula VII can be prepared by reacting a benzothiazole of the formula ##STR13## wherein X and n are as heretofore described, with phosgene. This reaction can be effected by adding a slurry or solution of the benzothiazole in a suitable organic solvent such as ethyl acetate to a solution of phosgene in a similar solvent. The resulting mixture can then be heated at reflux for a period of from 1/2to 2 hours. The desired product can then be recovered by filtration if formed as a precipitate or upon evaporation of the organic solvent if soluble therein.

Exemplary suitable compounds of formula VIII for preparing the compounds of the present invention are the dimethyl acetal of 2-methylaminoacetaldehyde, the dimethyl acetal of 2-ethylaminoacetaldehyde, the dimethyl acetal of 2-propylaminoacetaldehyde, the dimethyl acetal of 2-allylaminoacetaldehyde, the dimethyl acetal of 2-chloromethylaminoacetaldehyde, the dimethyl acetal of 2-β-bromoethylaminoacetaldehyde, the dimethyl acetal of 2-propargylaminoacetaldehyde and the like.

Exemplary suitable compounds of formula IX for preparing the compounds of this invention are 2-aminobenzothiazole, 2-amino-5-methylbenzothiazole, 2-amino-6-chlorobenzothiazole, 2-amino-4,5-dimethylbenzothiazole, 2-amino-7-bromobenzothiazole, 2-amino-6-methoxybenzothiazole, 2-amino-6-fluorobenzothiazole, 2-amino-4-methyl-6-chlorobenzothiazole, 2-amino-4-chloromethylbenzothiazole, 2-amino-5-β-bromoethylbenzothiazole, 2-amino-6-trifluoromethylbenzothiazole and the like.

Exemplary suitable compounds of formulae III and IV for preparing the compounds of the present invention are the acid chlorides or anhydrides of the following acids: acetic acid, propionic acid, butanoic acid, pentanoic acid, hexanoic acid, octanoic acid, dodecanoic acid, octadecanoic acid, acrylic acid, butenoic acid, pentenoic acid, chloroacetic acid, bromoacetic acid, β-chlorobutanoic acid, cyclohexylcarboxylic acid, cyclopropylcarboxylic acid, benzoic acid, toluic acid, 4-chlorobenzoic acid, 3-bromobenzoic acid, 4-fluorobenzoic acid, 4-methoxybenzoic acid, 4-ethoxybenzoic acid, 4-chloromethylbenzoic acid, 4-trifluoromethylbenzoic acid, 3,4,5-trichlorobenzoic acid, 3-methylthiobenzoic acid, 3-ethylthiobenzoic acid, 4-butylthiobenzoic acid, phenylacetic acid, β-phenylpropionic acid, 4-methylphenylacetic acid, propynoic acid, butynoic acid, methoxyacetic acid, β-methoxypropionic acid, γ-ethoxybutanoic acid and the like.

The manner in which the compounds of the present invention can be prepared is more specifically illustrated in the following examples.

EXAMPLE 1 Preparation of Benzothiazol-2-yl Isocyanate Dimer

A saturated solution of phosgene in ethyl acetate (1200 ml) is charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. 2-Aminobenzothiazole (100.0 grams; 0.67 mole) is then added with stirring. After the addition is completed, the reaction mixture is heated at reflux for a period of about 1 hour. After this time the reaction mixture is evaporated to dryness to yield the desired product benzothiazol-2-yl isocyanate dimer as a yellow solid having a melting point of 250° to 252° C.

EXAMPLE 2 Preparation of the Dimethyl Acetal of 2-(1-Methyl-3-benzothiazol-2-ylureido)acetaldehyde

Benzothiazol-2-yl isocyanate dimer prepared in Example 1, benzene (300 ml) and the dimethyl acetal of 2-methylaminoacetaldehyde (80 grams; 0.67 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred at room temperature for a period of about 1 hour. After this time the mixture is filtered to remove a yellow solid that has formed. The filtrate is then stripped of solvent under reduced pressure to yield the desired product the dimethyl acetal of 2-(1-methyl-3-benzothiazol-2-ylureido)acetaldehyde as an oil.

EXAMPLE 3 Preparation of 1-Benzothiazol-2-yl-3-methyl-5-hydroxy-1,3-imidazolidin-2-one

The dimethyl acetal of 2-(1-methyl-3-benzothiazol-2-ylureido)acetaldehyde (150 grams), methanol (750 ml), water (750 ml) and concentrated hydrochloric acid (75 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. The reaction mixture is blanketed with nitrogen gas and is heated at reflux for a period of about 15 minutes. After this time the mixture is stripped of most of the solvents, and the residue is combined with aqueous sodium bicarbonate (500 ml). The mixture is then extracted with ethyl acetate, and the resulting solution is dried over anhydrous magnesium sulfate. The dried solution is then stripped of solvent to yield the desired product 1-benzothiazol-2-yl-3-methyl-5-hydroxy-1,3-imidazolidin-2-one as a yellow solid melting at 168° to 170° C.

EXAMPLE 4 Preparation of 1-Benzothiazol-2-yl-3-methyl-5-acetyloxy-1,3-imidazolidin-2-one

1-Benzothiazol-2-yl-3-methyl-5-hydroxy-1,3-imidazolidin-2-one (0.1 mole), acetyl chloride (0.11 mole) and pyridine (0.11 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred for a period of about 15 minutes and is then allowed to stand for a period of about 2 hours. After this time water (100 ml) and hexane (30 ml) are added to the mixture. The organic phase is then separated from the aqueous phase and is dried over anhydrous magnesium sulfate. The dried solution is then filtered and stripped of solvent under reduced pressure to yield the desired product 1-benzothiazol-2-yl-3-methyl-5-acetyloxy-1,3-imidazolidin-2-one as the residue.

EXAMPLE 5 Preparation of 5-Methylbenzothiazol-2-yl Isocyanate Dimer

A saturated solution of phosgene in ethyl acetate (200 ml) is charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. 2-Amino-5-methylbenzothiazole (0.1 mole) is added with stirring. After the addition is completed, the reaction mixture is heated at reflux for a period of about 1 hour. After this time the mixture is cooled, and the solid product formed is recovered by filtration. The solid is then dried to yield the desired product 5-methylbenzothiazol-2-yl isocyanate dimer.

EXAMPLE 6 Preparation of the Dimethyl Acetal of 2-[1-Methyl-3-(5-methylbenzothiazol-2-yl)ureido]acetaldehyde

5-Methylbenzothiazol-2-yl isocyanate dimer (0.1 mole), the dimethyl acetal of 2-methylaminoacetaldehyde (0.2 mole) and benzene (100 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred at ambient temperatures for a period of about 1 hour. After this time the reaction mixture is filtered, and the filtrate is stripped of solvent to yield the desired product the dimethyl acetal of 2-[1-methyl-3-(5-methylbenzothiazol-2-yl)ureido]acetaldehyde as the residue.

EXAMPLE 7 Preparation of 1-(5-Methylbenzothiazol-2-yl)-3-methyl-5-hydroxy-1,3-imidazolidin-2-one

The dimethyl acetal of 2-[1-methyl-3-(5-methylbenzothiazol-2-yl)ureido]acetaldehyde (15 grams), water (200 ml), methanol (200 ml) and concentrated hydrochloric acid (10 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. The reaction mixture is heated at reflux for a period of about 15 minutes. After this time the reaction mixture is stripped of solvents under reduced pressure, leaving a residue. This residue is recrystallized to yield the desired product 1-(5-methylbenzothiazol-2-yl)-3-methyl-5-hydroxy-1,3-imidazolidin-2-one.

EXAMPLE 8 Preparation of 1-(5-Methylbenzothiazol-2-yl)-3-methyl-5-acryloyloxy-1,3-imidazolidin-2-one

1-(5-Methylbenzothiazol-2-yl)-3-methyl-5-hydroxy-1,3-imidazolidin-2-one (0.1 mole), acryloyl chloride (0.11 mole) and pyridine (0.11 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred for a period of about 15 minutes and is then allowed to stand for a period of about 2 hours. After this time water (100 ml) and hexane (30 ml) are added to the mixture. The organic phase is then separated from the aqueous phase and is dried over anhydrous magnesium sulfate. The dried solution is then filtered and stripped of solvent under reduced pressure to yield the desired product 1-(5-methylbenzothiazol-2-yl)-3-methyl-5-acryloyloxy-1,3-imidazolidin-2-one as the residue.

EXAMPLE 9 Preparation of 6-Chlorobenzothiazol-2-yl Isocyanate Dimer

A saturated solution of phosgene in ethyl acetate (200 ml) is charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. 2-Amino-6-chlorobenzothiazole (0.1 mole) is added with stirring. After the addition is completed, the reaction mixture is heated at reflux for a period of about 1 hour. After this time the mixture is cooled, and the solid product formed is recovered by filtration. The solid is then dried to yield the desired product 6-chlorobenzothiazol-2-yl isocyanate dimer.

EXAMPLE 10 Preparation of the Dimethyl Acetal of 2-[1-Allyl-3-(6-chlorobenzothiazol-2-yl)ureido]acetaldehyde

6-Chlorobenzothiazol-2-yl isocyanate dimer (0.1 mole), the dimethyl acetal of 2-allylaminoacetaldehyde (0.2 mole) and benzene (100 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred at ambient temperatures for a period of about 1 hour. After this time the reaction mixture is filtered, and the filtrate is stripped of solvent to yield the desired product the dimethyl acetal of 2-[1-allyl-3-(6-chlorobenzothiazol-2-yl)ureido]acetaldehyde as the residue.

EXAMPLE 11 Preparation of 1-(6-Chlorobenzothiazol-2-yl)-3-allyl-5-hydroxy-1,3-imidazolidin-2-one

The dimethyl acetal of 2-[1-allyl-3-(6-chlorobenzothiazol-2-yl)ureido]acetaldehyde (15 grams), water (200 ml), methanol (200 ml) and concentrated hydrochloric acid (10 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. The reaction mixture is heated at reflux for a period of about 15 minutes. After this time the reaction mixture is stripped of solvents under reduced pressure, leaving a residue. This residue is recrystallized to yield the desired product 1-(6-chlorobenzothiazol-2-yl)-3-allyl-5-hydroxy-1,3-imidazolidin-2-one.

EXAMPLE 12 Preparation of 1-(6-Chlorobenzothiazol-2-yl)-3-allyl-5-α-chloroacetyloxy-1,3-imidazolidin-2-one

1-(6-Chlorobenzothiazol-2-yl)-3-allyl-5-hydroxy-1,3-imidazolidin-2-one (0.1 mole), α-chloroacetyl chloride (0.11 mole) and pyridine (0.11 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred for a period of about 15 minutes and is then allowed to stand for a period of about 2 hours. After this time water (100 ml) and hexane (30 ml) are added to the mixture. The organic phase is then separated from the aqueous phase and is dried over anhydrous magnesium sulfate. The dried solution is then filtered and stripped of solvent under reduced pressure to yield the desired product 1-(6-chlorobenzothiazol-2-yl)-3-allyl-5-α-chloroacetyloxy-1,3-imidazolidin-2-one as the residue.

EXAMPLE 13 Preparation of 7-Bromobenzothiazol-2-yl Isocyanate Dimer

A saturated solution of phosgene in ethyl acetate (200 ml) is charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. 2-Amino-7-bromobenzothiazole (0.1 mole) is added with stirring. After this time the mixture is cooled, and the solid product formed is recovered by filtration. The solid is then dried to yield the desired product 7-bromobenzothiazol-2-yl isocyanate dimer.

EXAMPLE 14 Preparation of the Dimethyl Acetal of 2-[1-Propargyl-3-(7-bromobenzothiazol-2-yl)ureido]acetaldehyde

7-Bromobenzothiazol-2-yl isocyanate dimer (0.1 mole), the dimethyl acetal of 2-propargylaminoacetaldehyde (0.2 mole) and benzene (100 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred at ambient temperatures for a period of about 1 hour. After this time the reaction mixture is filtered, and the filtrate is stripped of solvent to yield the desired product the dimethyl acetal of 2-[1-propargyl-3-(7-bromobenzothiazol-2-yl)ureido]acetaldehyde as the residue.

EXAMPLE 15 Preparation of 1-(7-Bromobenzothiazol-2-yl)-3-propargyl-5-hydroxy-1,3-imidazolidin-2-one

The dimethyl acetal of 2-[1-propargyl-3-(7-bromobenzothiazol-2-yl)ureido]acetaldehyde (15 grams), water (200 ml), methanol (200 ml) and concentrated hydrochloric acid (10 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. The reaction mixture is heated at reflux for a period of about 15 minutes. After this time the reaction mixture is stripped of solvents under reduced pressure, leaving a residue. This residue is recrystallized to yield the desired product 1-(7-bromobenzothiazol-2-yl)-3-propargyl-5-hydroxy-1,3-imidazolidin-2-one.

EXAMPLE 16 Preparation of 1-(7-Bromobenzothiazol-2-yl)-3-propargyl-5-propynoyloxy-1,3-imidazolidin-2-one

1-(7-Bromobenzothiazol-2-yl)-3-propargyl-5-hydroxy-1,3-imidazolidin-2-one (0.1 mole), propynoyl chloride (0.11 mole) and pyridine (0.11 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred for a period of about 15 minutes and is then allowed to stand for a period of about 2 hours. After this time water (100 ml) and hexane (30 ml) are added to the mixture. The organic phase is then separated from the aqueous phase and is dried over anhydrous magnesium sulfate. The dried solution is then filtered and stripped of solvent under reduced pressure to yield the desired product 1-(7-bromobenzothiazol-2-yl)-3-propargyl-5-propynoyloxy-1,3-imidazolidin-2-one as the residue.

EXAMPLE 17 Preparation of 4-Methoxybenzothiazol-2-yl Isocyanate Dimer

A saturated solution of phosgene in ethyl acetate (200 ml) is charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. 2-Amino-4-methoxybenzothiazole (0.1 mole) is added with stirring. After the addition is completed, the reaction mixture is heated at reflux for a period of about 1 hour. After this time the mixture is cooled, and the solid product formed is recovered by filtration. The solid is then dried to yield the desired product 4-methoxybenzothiazol-2-yl isocyanate dimer.

EXAMPLE 18 Preparation of the Dimethyl Acetal of 2-[1-Ethyl-3-(4-methoxybenzothiazol-2-yl)ureido]acetaldehyde

4-Methoxybenzothiazol-2-yl isocyanate dimer (0.1 mole), the dimethyl acetal of 2-ethylaminoacetaldehyde (0.2 mole) and benzene (100 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred at ambient temperatures for a period of about 1 hour. After this time the reaction mixture is filtered, and the filtrate is stripped of solvent to yield the desired product the dimethyl acetal of 2-[1-ethyl-3-(4-methoxybenzothiazol-2-yl)ureido]acetaldehyde as the residue.

EXAMPLE 19 Preparation of 1-(4-Methoxybenzothiazol-2-yl)-3-ethyl-5-hydroxy-1,3-imidazolidin-2-one

The dimethyl acetal of 2-[1-ethyl-3-(4-methoxybenzothiazol-2-yl)ureido]acetaldehyde (15 grams), water (200 ml), methanol (200 ml) and concentrated hydrochloric acid (10 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. The reaction mixture is heated at reflux for a period of about 15 minutes. After this time the reaction mixture is stripped of solvents under reduced pressure, leaving a residue. This residue is recrystallized to yield the desired product 1-(4-methoxybenzothiazol-2-yl)-3-ethyl-5-hydroxy-1,3-imidazolidin-2-one.

EXAMPLE 20 Preparation of 1-(4-Methoxybenzothiazol-2-yl)-3-ethyl-5-α-methoxyacetyloxy-1,3-imidazolidin-2-one

1-(4-Methoxybenzothiazol-2-yl)-3-ethyl-5-hydroxy-1,3-imidazolidin-2-one (0.1 mole), α-methoxyacetyl chloride (0.11 mole) and pyridine (0.11 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred for a period of about 15 minutes and is then allowed to stand for a period of about 2 hours. After this time water (100 ml) and hexane (30 ml) are added to the mixture. The organic phase is then separated from the aqueous phase and is dried over anhydrous magnesium sulfate. The dried solution is then filtered and stripped of solvent under reduced pressure to yield the desired product 1-(4-methoxybenzothiazol-2-yl)-3-ethyl-5-α-methoxyacetyloxy-1,3-imidazolidin-2-one as the residue.

EXAMPLE 21 Preparation of 5-Fluorobenzothiazol-2-yl Isocyanate Dimer

A saturated solution of phosgene in ethyl acetate (200 ml) is charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. 2-Amino-5-fluorobenzothiazole (0.1 mole) is added with stirring. After the addition is completed, the reaction mixture is heated at reflux for a period of about 1 hour. After this time the mixture is cooled, and the solid product formed is recovered by filtration. The solid is then dried to yield the desired product 5-fluorobenzothiazol-2-yl isocyanate dimer.

EXAMPLE 22 Preparation of the Dimethyl Acetal of 2-[1-Chloromethyl-3-(5-fluorobenzothiazol-2-yl)ureido]acetaldehyde

5-Fluorobenzothiazol-2-yl isocyanate dimer (0.1 mole), the dimethyl acetal of 2-chloromethylaminoacetaldehyde (0.2 mole) and benzene (100 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred at ambient temperatures for a period of about 1 hour. After this time the reaction mixture is filtered, and the filtrate is stripped of solvent to yield the desired product the dimethyl acetal of 2-[1-chloromethyl-3-(5-fluorobenzothiazol-2-yl)ureido]acetaldehyde as the residue.

EXAMPLE 23 Preparation of 1-(5-Fluorobenzothiazol-2-yl)-3-chloromethyl-5-hydroxy-1,3-imidazolidin-2-one

The dimethyl acetal of 2-[1-chloromethyl-3-(5-fluorobenzothiazol-2-yl)ureido]acetaldehyde (15 grams), water (200 ml), methanol (200 ml) and concentrated hydrochloric acid (10 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. The reaction mixture is heated at reflux for a period of about 15 minutes. After this time the reaction mixture is stripped of solvents under reduced pressure, leaving a residue. This residue is recrystallized to yield the desired product 1-(5-fluorobenzothiazol-2-yl)-3-chloromethyl-5-hydroxy-1,3-imidazolidin-2-one.

EXAMPLE 24 Preparation of 1-(5-Fluorobenzothiazol-2-yl)-3-chloromethyl-5-cyclopropylcarbonyloxy-1,3-imidazolidin-2-one

1-(5-Fluorobenzothiazol-2-yl)-3-chloromethyl-5-hydroxy-1,3-imidazolidin-2-one (0.1 mole), cyclopropylcarboxylic acid chloride (0.11 mole) and pyridine (0.11 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred for a period of about 15 minutes and is then allowed to stand for a period of about 2 hours. After this time water (100 ml) and hexane (30 ml) are added to the mixture. The organic phase is then separated from the aqueous phase and is dried over anhydrous magnesium sulfate. The dried solution is then filtered and stripped of solvent under reduced pressure to yield the desired product 1-(5-fluorobenzothiazol-2-yl)-3-chloromethyl-5-cyclopropylcarbonyloxy-1,3-imidazolidin-2-one as the residue.

EXAMPLE 25 Preparation of 5-Trifluoromethylbenzothiazol-2-yl Isocyanate Dimer

A saturated solution of phosgene in ethyl acetate (200 ml) is charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. 2-Amino-5-trifluoromethylbenzothiazole (0.1 mole) is added with stirring. After the addition is completed, the reaction mixture is heated at reflux for a period of about 1 hour. After this time the mixture is cooled, and the solid product formed is recovered by filtration. The solid is then dried to yield the desired product 5-trifluoromethylbenzothiazol-2-yl isocyanate dimer.

EXAMPLE 26 Preparation of the Dimethyl Acetal of 2-[1-β-Bromoethyl-3-(5-trifluoromethylbenzothiazol-2-yl)ureido]acetaldehyde

5-Trifluoromethylbenzothiazol-2-yl isocyanate dimer (0.1 mole), the dimethyl acetal of 2-β-bromoethylaminoacetaldehyde (0.2 mole) and benzene (100 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred at ambient temperatures for a period of about 1 hour. After this time the reaction mixture is filtered, and the filtrate is stripped of solvent to yield the desired product the dimethyl acetal of 2-[1-β-bromoethyl-3-(5-trifluoromethylbenzothiazol-2-yl)ureido]acetaldehyde as the residue.

EXAMPLE 27 Preparation of 1-(5-Trifluoromethylbenzothiazol-2-yl)-3-β-bromoethyl-5-hydroxy-1,3-imidazolidin-2-one

The dimethyl acetal of 2-[1-β-bromoethyl-3-(5-trifluoromethylbenzothiazol-2-yl)ureido]acetaldehyde (15 grams), water (200 ml), methanol (200 ml) and concentrated hydrochloric acid (10 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. The reaction mixture is heated at reflux for a period of about 15 minutes. After this time the reaction mixture is stripped of solvents under reduced pressure, leaving a residue. This residue is recrystallized to yield the desired product 1-(5-trifluoromethylbenzothiazol-2-yl)-3-β-bromoethyl-5-hydroxy-1,3-imidazolidin-2-one.

EXAMPLE 28 Preparation of 1-(5-Trifluoromethylbenzothiazol-2-yl)-3-β-bromoethyl-5-benzoyloxy-1,3-imidazolidin-2-one

1-(5-Trifluoromethylbenzothiazol-2-yl)-3-β-bromoethyl-5-hydroxy-1,3-imidazolidin-2-one (0.1 mole), benzoyl chloride (0.11 mole) and pyridine (0.11 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred for a period of about 15 minutes and is then allowed to stand for a period of about 2 hours. After this time water (100 ml) and hexane (30 ml) are added to the mixture. The organic phase is then separated from the aqueous phase and is dried over anhydrous magnesium sulfate. The dried solution is then filtered and stripped of solvent under reduced pressure to yield the desired product 1-(5-trifluoromethylbenzothiazol-2-yl)-3-β-bromoethyl-5-benzoyloxy-1,3-imidazolidin-2-one as the residue.

EXAMPLE 29 Preparation of 1-Benzothiazol-2-yl-3-methyl-5-benzoyloxy-1,3-imidazolidin-2-one

1-Benzothiazol-2-yl-3-methyl-5-hydroxy-1,3-imidazolidin-2-one (0.1 mole), benzoyl chloride (0.11 mole) and pyridine (0.11 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred for a period of about 15 minutes and is then allowed to stand for a period of about 2 hours. After this time water (100 ml) and hexane (30 ml) are added to the mixture. The organic phase is then separated from the aqueous phase and is dried over anhydrous magnesium sulfate. The dried solution is then filtered and stripped of solvent under reduced pressure to yield the desired product 1-benzothiazol-2-yl-3-methyl-5-benzoyloxy-1,3-imidazolidin-2-one as the residue.

EXAMPLE 30 Preparation of 1-Benzothiazol-2-yl-3-methyl-5-(4-chlorobenzoyloxy)-1,3-imidazolidin-2-one

1-Benzothiazol-2-yl-3-methyl-5-hydroxy-1,3-imidazolidin-2-one (0.1 mole), 4-chlorobenzoyl chloride (0.11 mole) and pyridine (0.11 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred for a period of about 15 minutes and is then allowed to stand for a period of about 2 hours. After this time water (100 ml) and hexane (30 ml) are added to the mixture. The organic phase is then separated from the aqueous phase and is dried over anhydrous magnesium sulfate. The dried solution is then filtered and stripped of solvent under reduced pressure to yield the desired product 1-benzothiazol-2-yl-3-methyl-5-(4-chlorobenzoyloxy)-1,3-imidazolidin-2-one as the residue.

EXAMPLE 31 Preparation of 1-Benzothiazol-2-yl-3-methyl-5-(2-methylbenzoyloxy)-1,3-imidazolidin-2-one

1-Benzothiazol-2-yl-3-methyl-5-hydroxy-1,3-imidazolidin-2-one (0.1 mole), 2-methylbenzoyl chloride (0.11 mole) and pyridine (0.11 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred for a period of about 15 minutes and is then allowed to stand for a period of about 2 hours. After this time water (100 ml) and hexane (30 ml) are added to the mixture. The organic phase is then separated from the aqueous phase and is dried over anhydrous magnesium sulfate. The dried solution is then filtered and stripped of solvent under reduced pressure to yield the desired product 1-benzothiazol-2-yl-3-methyl-5-(2-methylbenzoyloxy)-1,3-imidazolidin-2-one as the residue.

EXAMPLE 32 Preparation of 1-Benzothiazol-2-yl-3-methyl-5-(3-allylbenzoyloxy)-1,3-imidazolidin-2-one

1-Benzothiazol-2-yl-3-methyl-5-hydroxy-1,3-imidazolidin-2-one (0.1 mole), 3-allylbenzoyl chloride (0.11 mole) and pyridine (0.11 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred for a period of about 15 minutes and is then allowed to stand for a period of about 2 hours. After this time water (100 ml) and hexane (30 ml) are added to the mixture. The organic phase is then separated from the aqueous phase and is dried over anhydrous magnesium sulfate. The dried solution is then filtered and stripped of solvent under reduced pressure to yield the desired product 1-benzothiazol-2-yl-3-methyl-5-(3-allylbenzoyloxy)-1,3-imidazolidin-2-one.

EXAMPLE 33 Preparation of 1-Benzothiazol-2-yl-3-methyl-5-(4-trifluoromethylbenzoyloxy)-1,3-imidazolidin-2-one

1-Benzothiazol-2-yl-3-methyl-5-hydroxy-1,3-imidazolidin-2-one (0.1 mole), 4-trifluoromethylbenzoyl chloride (0.11 mole) and pyridine (0.11 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred for a period of about 15 minutes and is then allowed to stand for a period of about 2 hours. After this time water (100 ml) and hexane (30 ml) are added to the mixture. The organic phase is then separated from the aqueous phase and is dried over anhydrous magnesium sulfate. The dried solution is then filtered and stripped of solvent under reduced pressure to yield the desired product 1-benzothiazol-2-yl-3-methyl-5-(4-trifluoromethylbenzoyloxy)-1,3-imidazolidin-2-one as the residue.

EXAMPLE 34 Preparation of 1-Benzothiazol-2-yl-3-methyl-5-(2,6-dimethoxybenzoyloxy)-1,3-imidazolidin-2-one

1-Benzothiazol-2-yl-3-methyl-5-hydroxy-1,3-imidazolidin-2-one (0.1 mole), 2,6-dimethoxybenzoyl chloride (0.11 mole) and pyridine (0.11 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred for a period of about 15 minutes and is then allowed to stand for a period of about 2 hours. After this time water (100 ml) and hexane (30 ml) are added to the mixture. The organic phase is then separated from the aqueous phase and is dried over anhydrous magnesium sulfate. The dried solution is then filtered and stripped of solvent under reduced pressure to yield the desired product 1-benzothiazol-2-yl-3methyl-5-(2,6-dimethoxybenzoyloxy)-1,3-imidazolidin-2-one as the residue.

EXAMPLE 35 Preparation of 1-Benzothiazol-2-yl-3-methyl-5-(3-methylthiobenzoyloxy)-1,3-imidazolidin-2-one

1-Benzothiazol-2-yl-3-methyl-5-hydroxy-1,3-imidazolidin-2-one (0.1 mole), 3-methylthiobenzoyl chloride (0.11 mole) and pyridine (0.11 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred for a period of about 15 minutes and is then allowed to stand for a period of about 2 hours. After this time water (100 ml) and hexane (30 ml) are added to the mixture. The organic phase is then separated from the aqueous phase and is dried over anhydrous magnesium sulfate. The dried solution is then filtered and stripped of solvent under reduced pressure to yield the desired product 1-benzothiazol-2-yl-3-methyl-5-(3-methylthiobenzoyloxy)-1,3-imidazolidin-2-one as the residue.

EXAMPLE 36 Preparation of 1-Benzothiazol-2-yl-3-methyl-5-(3-nitrobenzoyloxy)-1,3-imidazolidin-2-one

1-Benzothiazol-2-yl-3-methyl-5-hydroxy-1,3-imidazolidin-2-one (0.1 mole), 3-nitrobenzoyl chloride (0.11 mole) and pyridine (0.11 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred for a period of about 15 minutes and is then allowed to stand for a period of about 2 hours. After this time water (100 ml) and hexane (30 ml) are added to the mixture. The organic phase is then separated from the aqueous phase and is dried over anhydrous magnesium sulfate. The dried solution is then filtered and stripped of solvent under reduced pressure to yield the desired product 1-benzothiazol-2-yl-3-methyl-5-(3-nitrobenzoyloxy)-1,3-imidazolidin-2-one as the residue.

EXAMPLE 37 Preparation of 1-Benzothiazol-2-yl-3-methyl-5-(4-cyanobenzoyloxy)-1,3-imidazolidin-2-one

1-Benzothiazol-2-yl-3-methyl-5-hydroxy-1,3-imidazolidin-2-one (0.1 mole), 4-cyanobenzoyl chloride (0.11 mole) and pyridine (0.11 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred for a period of about 15 minutes and is then allowed to stand for a period of about 2 hours. After this time water (100 ml) and hexane (30 ml) are added to the mixture. The organic phase is then separated from the aqueous phase and is dried over anhydrous magnesium sulfate. The dried solution is then filtered and stripped of solvent under reduced pressure to yield the desired product 1-benzothiazol-2-yl-3-methyl-5-(4-cyanobenzoyloxy)-1,3-imidazolidin-2-one as the residue.

EXAMPLE 38 Preparation of 1-Benzothiazol-2-yl-3-methyl-5-phenylacetyloxy-1,3-imidazolidin-2-one

1-Benzothiazol-2-yl-3-methyl-5-hydroxy-1,3-imidazolidin-2-one (0.1 mole), phenylacetyl chloride (0.11 mole) and pyridine (0.11 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred for a period of about 15 minutes and is then allowed to stand for a period of about 2 hours. After this time water (100 ml) and hexane (30 ml) are added to the mixture. The organic phase is then separated from the aqueous phase and is dried over anhydrous magnesium sulfate. The dried solution is then filtered and stripped of solvent under reduced pressure to yield the desired product 1-benzothiazol-2-yl-3-methyl-5-phenylacetyloxy-1,3-imidazolidin-2-one as the residue.

EXAMPLE 39 Preparation of 1-Benzothiazol-2-yl-3-methyl-5-[β-(3,4-dichlorophenyl)-propionyloxy]-1,3-imidazolidin-2-one

1-Benzothiazol-2-yl-3-methyl-5-hydroxy-1,3-imidazolidin-2-one (0.1 mole), β-(3,4-dichlorophenyl)propionyl chloride (0.11 mole) and pyridine (0.11 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred for a period of about 15 minutes and is then allowed to stand for a period of about 2 hours. After this time water (100 ml) and hexane (30 ml) are added to the mixture. The organic phase is then separated from the aqueous phase and is dried over anhydrous magnesium sulfate. The dried solution is then filtered and stripped of solvent under reduced pressure to yield the desired product 1-benzothiazol-2-yl-3-methyl-5-[β-(3,4-dichlorophenyl)-propionyloxy]-1,3-imidazolidin-2-one as the residue.

EXAMPLE 40 Preparation of 1-Benzothiazol-2-yl-3-methyl-5-cyclohexylcarbonyloxy-1,3-imidazolidin-2-one

1-Benzothiazol-2-yl-3-methyl-5-hydroxy-1,3-imidazolidin-2-one (0.1 mole), cyclohexylcarboxylic acid chloride (0.11 mole) and pyridine (0.11 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred for a period of about 15 minutes and is then allowed to stand for a period of about 2 hours. After this time water (100 ml) and hexane (30 ml) are added to the mixture. The organic phase is then separated from the aqueous phase and is dried over anhydrous magnesium sulfate. The dried solution is then filtered and stripped of solvent under reduced pressure to yield the desired product 1-benzothiazol-2-yl-3-methyl-5-cyclohexylcarbonyloxy-1,3-imidazolidin-2-one as the residue.

Additional compounds within the scope of the present invention which can be prepared according to the procedures of the foregoing examples include 1-(4-ethylbenzothiazol-2-yl)-3-ethyl-5-propanoyloxy-1,3-imidazolidin-2-one, 1-(5-propylbenzothiazol-2-yl)-3-propyl-5-butanoyloxy-1,3-imidazolidin-2-one, 1-(6-butylbenzothiazol-2-yl)-3-butyl-5-pentanoyloxy-1,3-imidazolidin-2-one, 1-(4-pentylbenzothiazol-2-yl)-3-pentyl-5-hexanoyloxy-1,3-imidazolidin-2-one, 1-(5-hexylbenzothiazol-2-yl)-3-hexyl-5-octanoyloxy-1,3-imidazolidin-2-one, 1-(6-allylbenzothiazol-2-yl)-3-but-3-enyl-5-nonanoyloxy-1,3-imidazolidin-2-one, 1-(4-but-3-enylbenzothiazol-2-yl)-3-pent-3-enyl-5-dodecanoyloxy-1,3-imidazolidin-2-one, 1-(5-pent-4-enylbenzothiazol-2-yl)-3-hex-5-enyl-5-octadecanoyloxy-1,3-imidazolidin-2-one, 1-(6-hex-4-enylbenzothiazol-2-yl)-3-propargyl-5-but-3-enoyloxy-1,3-imidazolidin-2-one, 1-(4-methoxybenzothiazol-2-yl)-3-but-2-ynyl-5-pent-4-enoyloxy-1,3-imidazolidin-2-one, 1-(5-ethoxybenzothiazol-2-yl)-3-pent-4-ynyl-5-hex-5-enoyloxy-1,3-imidazolidin-2-one, 1-(6-butoxybenzothiazol-2-yl)-3-β-chloroethyl-5-bromoacetyloxy-1,3-imidazolidin-2-one, 1-(4-pentyloxybenzothiazol-2-yl)-3-γ-bromopropyl-5-β-bromopropanoyloxy-1,3-imidazolidin-2-one, 1-(5-hexyloxybenzothiazol-2-yl)-3-β-bromopentyl-5-γ-chlorobutanoyloxy-1,3-imidazolidin-2-one, 1-(5-chloromethylbenzothiazol-2-yl)-3-ω-chlorohexyl-5-ethoxyacetyloxy-1,3-imidazolidin-2-one, 1-(5-β-chloroethylbenzothiazol-2-yl)-3-methyl-5-propoxyacetyloxy-1,3-imidazolidin-2-one, 1-(5-γ-bromopropylbenzothiazol-2-yl)-3-methyl-5-butoxyacetyloxy-1,3-imidazolidin-2-one, 1-(6-β-bromopentylbenzothiazol-2-yl)-3-methyl-5-δ-methoxybutanoyloxy-1,3-imidazolidin-2-one, 1-benzothiazol-2-yl-3-methyl-5-(2-ethylbenzoyloxy)-1,3-imidazolidin-2-one, 1-benzothiazol-2-yl-3-methyl-5-(2-propylbenzoyloxy)-1,3-imidazolidin-2-one, 1-benzothiazol-2-yl-3-methyl-5-(3-butylbenzoyloxy)-1,3-imidazolidin-2-one, 1-benzothiazol-2-yl-3-methyl-5-(3-hexylbenzoyloxy)-1,3-imidazolidin-2-one, 1-benzothiazol-2-yl-3-methyl-5-(4-but-3-enylbenzoyloxy)-1,3-imidazolidin-2-one, 1-benzothiazol-2-yl-3-methyl-5-(4-hex-4-enylbenzoyloxy)-1,3-imidazolidin-2-one, 1-benzothiazol-2-yl-3-methyl-5-(4-bromobenzoyloxy)-1,3-imidazolidin-2-one, 1-benzothiazol-2-yl-3-methyl-5-(2,6-difluorobenzoyloxy)-1,3-imidazolidin-2-one, 1-benzothiazol-2-yl-3-methyl-5-(3-iodobenzoyloxy)-1,3-imidazolidin-2-one, 1-benzothiazol-2-yl-3-methyl-5-(4-ethoxybenzoyloxy)-1,3-imidazolidin-2-one, 1-benzothiazol-2-yl-3-methyl-5-(3-butoxybenzoyloxy)-1,3-imidazolidin-2-one, 1-benzothiazol-2-yl-3-methyl-5-(4-hexyloxybenzoyloxy)-1,3-imidazolidin-2-one, 1-benzothiazol-2-yl-3-methyl-5-(3-ethylthiobenzoyloxy)-1,3-imidazolidin-2-one, 1-benzothiazol-2-yl-3-methyl-5-(4-butylthiobenzoyloxy)-1,3-imidazolidin-2-one, 1-benzothiazol-2-yl-3-methyl-5-(2-hexylthiobenzoyloxy)-1,3-imidazolidin-2-one and the like.

For practical use as herbicides the compounds of this invention are generally incorporated into herbicidal compositions which comprise an inert carrier and a herbicidally toxic amount of such a compound. Such herbicidal compositions, which can also be called formulations, enable the active compound to be applied conveniently to the site of the weed infestation in any desired quantity. These compositions can be solids such as dusts, granules, or wettable powders; or they can be liquids such as solutions, aerosols, or emulsifiable concentrates.

For example, dusts can be prepared by grinding and blending the active compound with a solid inert carrier such as the talcs, clays, silicas, pyrophyllite, and the like. Granular formulations can be prepared by impregnating the compound, usually dissolved in a suitable solvent, onto and into granulated carriers such as the attapulgites or the vermiculites, usually of a particle size range of from about 0.3 to 1.5 mm. Wettable powders, which can be dispersed in water or oil to any desired concentration of the active compound, can be prepared by incorporating wetting agents into concentrated dust compositions.

In some cases the active compounds are sufficiently soluble in common organic solvents such as kerosene or xylene so that they can be used directly as solutions in these solvents. Frequently, solutions of herbicides can be dispersed under super-atmospheric pressure as aerosols. However, preferred liquid herbicidal compositions are emulsifiable concentrates, which comprise an active compound according to this invention and as the inert carrier, a solvent and an emulsifier. Such emulsifiable concentrates can be extended with water and/or oil to any desired concentration of active compound for application as sprays to the site of the weed infestation. The emulsifiers most commonly used in these concentrates are nonionic or mixtures of nonionic with anionic surface-active agents. With the use of some emulsifier systems an inverted emulsion (water in oil) can be prepared for direct application to weed infestations.

A typical herbicidal composition according to this invention is illustrated by the following example, in which the quantities are in parts by weight.

EXAMPLE 41

    ______________________________________                                         Preparation of a Dust                                                          ______________________________________                                         Product of Example 4      10                                                   Powdered Talc             90                                                   ______________________________________                                    

The above ingredients are mixed in a mechanical grinder-blender and are ground until a homogeneous, free-flowing dust of the desired particle size is obtained. This dust is suitable for direct application to the site of the weed infestation.

The compounds of this invention can be applied as herbicides in any manner recognized by the art. One method for the control of weeds comprises contacting the locus of said weeds with a herbicidal composition comprising an inert carrier and as an essential active ingredient, in a quantity which is herbicidally toxic to said weeds, a compound of the present invention. The concentration of the new compounds of this invention in the herbicidal compositions will vary greatly with the type of formulation and the purpose for which it is designed, but generally the herbicidal compositions will comprise from about 0.05 to about 95 percent by weight of the active compounds of this invention. In a preferred embodiment of this invention, the herbicidal compositions will comprise from about 5 to about 75 percent by weight of the active compound. The compositions can also comprise such additional substances as other pesticides, such as insecticides, nematocides, fungicides, and the like; stabilizers, spreaders, deactivators, adhesives, stickers, fertilizers, activators, synergists, and the like.

The compounds of the present invention are also useful when combined with other herbicides and/or defoliants, dessicants, growth inhibitors, and the like in the herbicidal compositions heretofore described. These other materials can comprise from about 5% to about 95% of the active ingredients in the herbicidal compositions. Use of combinations of these other herbicides and/or defoliants, dessicants, etc. with the compounds of the present invention provide herbicidal compositions which are more effective in controlling weeds and often provide results unattainable with separate compositions of the individual herbicides. The other herbicides, defoliants, dessicants and plant growth inhibitors, with which the compounds of this invention can be used in the herbicidal compositions to control weeds, can include chlorophenoxy herbicides such as 2,4-D, 2,4,5-T, MCPA, MCPB, 4(2,4-DB), 2,4-DEB, 4-CPB, 4-CPA, 4-CPP, 2,4,5-TB, 2,4,5-TES, 3,4-DA, silvex and the like; carbamate herbicides such as IPC, CIPC, swep, barban, BCPC, CEPC, CPPC, and the like; thiocarbamate and dithiocarbamate herbicides such as CDEC, metham sodium, EPTC, diallate, PEBC, perbulate, vernolate and the like; substituted urea herbicides such as norea, siduron, dichloral urea, chloroxuron, cycluron, fenuron, monuron, monuron TCA, diuron, linuron, monolinuron, neburon, buturon, trimeturon and the like; symmetrical triazine herbicides such as simazine, chlorazine, atraone, desmetryne, norazine, ipazine, prometryn, atrazine, trietazine, simetone, prometone, propazine, ametryne and the like; chloroacetamide herbicides such as alpha-chloro-N,N-dimethylacetamide, CDEA, CDAA, alpha-chloro-N-isopropylacetamide, 2-chloro-N-isopropylacetanilide, 4-(chloroacetyl)morpholine, 1-(chloroacetyl)piperidine and the like; chlorinated aliphatic acid herbicides such as TCA, dalapon, 2,3-dichloropropionic acid, 2,2,3-TPA and the like; chlorinated benzoic acid and phenylacetic acid herbicides such as 2,3,6-TBA, 2,3,5,6-TBA, dicamba, tricamba, amiben, fenac, PBA, 2-methoxy-3,6-dichlorophenylacetic acid, 3-methoxy-2,6-dichlorophenylacetic acid, 2-methoxy-3,5,6-trichlorophenylacetic acid, 2,4-dichloro-3-nitrobenzoic acid and the like; and such compounds as aminotriazole, maleic hydrazide, phenyl mercuric acetate, endothal, biuret, technical chlordane, dimethyl 2,3,5,6-tetrachloroterephthalate, diquat, erbon, DNC, DNBP, dichlobenil, DPA, diphenamid, dipropalin, trifluralin, solan, dicryl, merphos, DMPA, DSMA, MSMA, potassium azide, acrolein, benefin, bensulide, AMS, bromacil, 2-(3,4-dichlorophenyl)-4-methyl-1,2,4-oxadiazolidine-3,5-dione, bromoxynil, cacodylic acid, CMA, CPMF, cypromid, DCB, DCPA, dichlone, diphenatril, DMTT, DNAP, EBEP, EXD, HCA, ioxynil, IPX, isocil, potassium cyanate, MAA, MAMA, MCPES, MCPP, MH, molinate, NPA, OCH, paraquat, PCP, picloram, DPA, PCA, pyrichlor, sesone, terbacil, terbutol, TCBA, brominil, CP-50144, H-176-1, H-732, M-2901, planavin, sodium tetraborate, calcium cyanamid, DEF, ethyl xanthogen disulfide, sindone, sindone B, propanil and the like. Such herbicides can also be used in the methods and compositions of this invention in the form of their salts, esters, amides, and other derivatives whenever applicable to the particular parent compounds.

Weeds are undesirable plants growing where they are not wanted, having no economic value, and interfering with the production of cultivated crops, with the growing of ornamental plants, or with the welfare of livestock. Many types of weeds are known, including annuals such as pigweed, lambsquarters, foxtail, crabgrass, wild mustard, field pennycress, ryegrass, goose grass, chickweed, wild oats, velvet-leaf, purslane, barnyardgrass, smartweed, knotweed, cocklebur, wild buckwheat, kochia, medic, corn cockle, ragweed, sow-thistle, coffeeweed, croton, cuphea, dodder, fumitory, groundsel, hemp nettle, knawel, spurge, spurry, emex, jungle rice, pondweed, dog fennel, carpetweed, morningglory, bedstraw, ducksalad, naiad, cheatgrass, fall panicum, jimsonweed, witchgrass, switchgrass, watergrass, teaweed, wild turnip and sprangletop; biennials such as wild carrot, matricaria, wild barley, campion, chamomile, burdock, mullein, round-leaved mallow, bull thistle, hounds-tongue, moth mullein and purple star thistle; or perennials such as white cockle, perennial ryegrass, quackgrass, Johnsongrass, Canada thistle, hedge bindweed, Bermuda grass, sheep sorrel, curly dock, nutgrass, field chickweed, dandelion, campanula, field bindweed, Russian knapweed, mesquite, toadflax, yarrow, aster, gromwell, horsetail, ironweed, sesbania, bulrush, cattail, winter-cress, horsenettle, nutsedge, milkweed and sicklepod.

Similarly, such weeds can be classified as broadleaf or grassy weeds. It is economically desirable to control the growth of such weeds without damaging beneficial plants or livestock.

The new compounds of this invention are particularly valuable for weed control because they are toxic to many species and groups of weeds while they are relatively non-toxic to many beneficial plants. The exact amount of compound required will depend on a variety of factors, including the hardiness of the particular weed species, weather, type of soil, method of application, the kind of beneficial plants in the same area and the like. Thus, while the application of up to only about one or two ounces of active compound per acre may be sufficient for good control of a light infestation of weeds growing under adverse conditions, the application of 10 pounds or more of an active compound per acre may be required for good control of a dense infestation of hardy perennial weeds growing under favorable conditions.

The herbicidal toxicity of the new compounds of this invention can be demonstrated by the following established testing techniques known to the art, pre- and post-emergence testing.

The herbicidal activity of the compounds of this invention can be demonstrated by experiments carried out for the pre-emergence control of a variety of weeds. In these experiments small plastic greenhouse pots filled with dry soil are seeded with the various weed seeds. Twenty-four hours or less after seeding the pots are sprayed with water until the soil is wet and a test compound formulated as an aqueous emulsion of an acetone solution containing emulsifiers is sprayed at the desired concentrations on the surface of the soil.

After spraying, the soil containers are placed in the greenhouse and provided with supplementary heat as required and daily or more frequent watering. The plants are maintained under these conditions for a period of from 15 to 21 days, at which time the condition of the plants and the degree of injury to the plants is rated on a scale of from 0 to 10, as follows: 0 = no injury, 1,2 = slight injury, 3,4 = moderate injury, 5,6 = moderately severe injury, 7,8,9 = severe injury and 10 = death.

The herbicidal activity of the compounds of this invention can also be demonstrated by experiments carried out for the post-emergence control of a variety of weeds. In these experiments the compounds to be tested are formulated as aqueous emulsions and sprayed at the desired dosage on the foliage of the weeds that have attained a prescribed size. After spraying the plants are placed in a greenhouse and watered daily or more frequently. Water is not applied to the foliage of the treated plants. The severity of the injury is determined 10 to 15 days after treatment and is rated on the scale of from 0 to 10 heretofore described. 

We claim:
 1. A compound of the formula ##STR14##wherein X is selected from the group consisting of lower alkyl, chlorine, bromine, fluorine, lower chloroalkyl, lower bromoalkyl, trifluoromethyl, and lower alkoxy; n is an integer from 0 to 2; R¹ is selected from the group consisting of lower alkyl, lower alkenyl, lower haloalkyl and propargyl; and R² is selected from the group consisting of alkyl, of up to 18 carbon atoms, lower alkenyl, lower haloalkyl, propargyl, lower alkoxyalkyl, cycloalkyl of from 3 to 7 carbon atoms and ##STR15##wherein p is an integer from 0 to 2; Y is selected from the group consisting of lower alkyl, lower alkenyl, chlorine, bromine, fluorine lower haloalkyl, lower alkoxy, lower alkylthio, nitro and cyano; and m is an integer from 0 to
 3. 2. The compound of claim 1, 1-benzothiazol-2-yl-3-methyl-5-acetyloxy-1,3-imidazolidin-2-one.
 3. The compound of claim 1, 1-(5-methylbenzothiazol-2-yl)-3-methyl-5-acryloyloxy-1,3-imidazolidin-2-one.
 4. The compound of claim 1, 1-(6-chlorobenzothiazol-2-yl)-3-allyl-5-α-chloroacetyloxy-1,3-imidazolidin-2-one.
 5. The compound of claim 1, 1-(7-bromobenzothiazol-2-yl)-3-propargyl-5-propynoyloxy-1,3-imidazolidin-2-one.
 6. The compound of claim 1, 1-(4-methoxybenzothiazol-2-yl)-3-ethyl-5-α-methoxyacetyloxy-1,3-imidazolidin-2-one.
 7. The compound of claim 1, 1-(5-fluorobenzothiazol-2-yl)-3-chloromethyl-5-cyclopropylcarbonyloxy-1,3-imidazolidin-2-one.
 8. The compound of claim 1, 1-(5-trifluoromethylbenzothiazol-2-yl)-3-β-bromoethyl-5-benzoyloxy-1,3-imidazolidin-2-one.
 9. The compound of claim 1, 1-benzothiazol-2-yl-3-methyl-5-benzoyloxy-1,3-imidazolidin-2-one. 